Purity Veterinary Medicine Kitasamycin Tartrate API Kitasamycin Tartrate

• Customization: Available
• CAS No.: 39405-35-1
• Formula: C40h67no18
• Model NO.: QS-Kitasamycin Tartrate
• EINECS: 253-442-3
• Packaging Material: Negotiable
• Storage Method: Normal
• Shelf Life: >12 Months
• Nutrient Composition: Kitasamycin Tartrate
• Resource: Kitasamycin Tartrate
• The content of active substances: >99%
• Product Name: Kitasamycin Tartrate
• Name: Kitasamycin Tartrate Powder
• Appearance: White Powder
• Colour: White
• Grade: Pharmaceutical Grade
• Assay: >99%
• Application: API
• Specific: COA
• Test Method: HPLC
• Density: 1.25
• Mf: C35h59no13
• MW: 701.84186
• Psa: 193.91000
• Refractive Index: 1.532
• Logp: 0.84560
• Transport Package: Negotiable
• Specification: >99%
• Trademark: QS-Kitasamycin Tartrate
• Origin: Xian
• Production Capacity: 1000kg/Month

Product Description

Purity Veterinary Medicine Kitasamycin Tartrate API Kitasamycin Tartrate

Product Description

Product Details

Product Name	Kitasamycin
Appearance	Kitasamycin Powder
Assay	>99%
MW	701.84186
MF	C35H59NO13
fractive index	1.532
LOGP	0.84560

Venlafaxine is an antidepressant that belongs to serotonin and norepinephrine reuptake inhibitors (SNRIs). It can increase swimming and climbing behavior in rats during forced swimming tests, demonstrating antidepressant effects.
Application
Kitasamycin is an antibiotic medicine. Mainly applied in pigs feed, chickens' feed and cows' feed. It can elevate feed conversion rate, stimulate growth of young animals and increase culture benefits. Prevention of infectious respiratory diseases of livestock and poultry caused by G+bacteria, curenecrotic enteritis and decrease occurrence rate of intestinal diseases.

Application&Function

Venlafaxine works by inhibiting the reuptake of serotonin (5-HT) and norepinephrine (NA), and also has a certain inhibitory effect on the reuptake of dopamine. It has no affinity for cholinergic receptors, histamine receptors, and α 2 receptors in vitro. Venlafaxine is well absorbed in the gastrointestinal tract and is mainly metabolized by the cytochrome P450 1A2 enzyme in the liver. The half-life of the main active metabolite is 5-11 hours, and it usually reaches a steady-state concentration after 3 weeks.

Specification